| Term Name: | lissencephaly 10 |
|---|---|
| Synonyms: | LIS10 |
| Definition: | A lissencephaly characterized by variably delayed development, mildly to moderately impaired intellectual development and language delay, seizures, brain features consistent with neuronal migration defects that has_material_basis_in heterozygous mutation in the CEP85L gene on chromosome 6q22.31. |
| Ontology: | Human Disease [DOID:0112229] ( DOID:0112229 ) |